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1.
Materials (Basel) ; 12(18)2019 Sep 11.
Article in English | MEDLINE | ID: mdl-31514358

ABSTRACT

In recent years, the development of nuclear grade FeCrAl-based alloys with enhanced accident tolerance has been carried out for light water reactor (LWR) fuel cladding to serve as a substitute for zirconium-based alloys. To achieve excellent microstructure stability and mechanical properties, the control of precipitation particles is critical for application of FeCrAl-based alloys. In this paper, the effect of thermomechanical processing on the microstructure and precipitation behavior of hot-rolled FeCrAl alloy plates was examined. After hot rolling, the FeCrAl alloy plates had typical deformation textures. The rolling direction (RD) orientation gradually rotated from <100> to <110> along with increasing reduction. Shear bands and cell structures were formed in the matrix, and the former acted as preferable nucleation sites for crystallization. Improved deformation helped to produce strain-induced precipitation. The plate with 83% reduction had the most homogeneous and finest precipitation particles. Identification results by TEM indicated that the Laves precipitation was of the Fe2Nb-type crystal structure type, with impurities including Mo, Cr, and Si. The plate with uniform Laves particles displayed favorable heat stability after a long period of aging at 800 °C. The microstructure evolution of the aged sample was also observed. The deformation microstructure and the strain-induced precipitation mechanism of FeCrAl alloys are discussed.

2.
Invest Ophthalmol Vis Sci ; 60(1): 113-122, 2019 01 02.
Article in English | MEDLINE | ID: mdl-30629726

ABSTRACT

Purpose: To develop a culture regime for the in vitro human lens capsular bag model that better reflects clinical events following cataract surgery and to use this refined model to evaluate the putative impact of IOLs on PCO formation. Methods: Capsulorhexis and lens extraction were performed on human donor eyes to generate capsular bags attached to the ciliary body by the zonules. Preparations were secured by pinning the ciliary body to a silicone ring and maintaining in 6 mL serum-free EMEM for 28 days or in a graded culture system (days 1-3, 5% human serum and 10 ng/mL TGFß2; days 4-7, 2% human serum and 1 ng/mL TGFß2; days 8-14, 1% human serum and 0.1 ng/mL TGFß2; days 15-28, serum-free EMEM), which better mimics clinical changes. Preparations were monitored with phase-contrast and modified-dark-field microscopy. Cell coverage and light scatter were quantified using image analysis software. The transdifferentiation marker, α-SMA and matrix component, fibronectin were assessed by immunocytochemistry. To assess IOLs in the model, Alcon Acrysof or Hoya Vivinex IOLs were implanted in match-paired capsular bags. Results: Match-paired experiments showed that graded culture enhanced growth, facilitated matrix contraction, increased transdifferentiation, and promoted matrix deposition relative to serum-free culture. The graded culture protocol was applied to match-paired bags implanted with a Hoya Vivinex or an Alcon Acrysof IOL. The Vivinex demonstrated a lag in growth across the posterior capsule. However, by day 28, coverage was similar, but light-scatter was greater with Acrysof implanted. Cell growth on the Acrysof IOL anterior surface was significantly greater than Vivinex. Conclusions: The graded culture human capsular bag model serves as an excellent system to evaluate and develop intraocular lenses. The Hoya Vivinex IOL showed an overall better level of performance against postsurgical wound healing and PCO than the Alcon Acrysof using this model.


Subject(s)
Capsule Opacification/etiology , Lens Capsule, Crystalline/physiology , Lens Implantation, Intraocular/adverse effects , Lenses, Intraocular , Models, Biological , Posterior Capsule of the Lens/pathology , Actins/metabolism , Adult , Aged , Aged, 80 and over , Capsule Opacification/pathology , Cell Movement/physiology , Cell Proliferation/physiology , Cell Transdifferentiation/physiology , Epithelial Cells/metabolism , Epithelial Cells/pathology , Female , Fibronectins/metabolism , Fluorescent Antibody Technique, Indirect , Humans , Light , Male , Middle Aged , Myofibroblasts/metabolism , Myofibroblasts/pathology , Organ Culture Techniques , Scattering, Radiation , Tissue Donors
3.
Materials (Basel) ; 11(11)2018 Nov 13.
Article in English | MEDLINE | ID: mdl-30428609

ABSTRACT

As leading candidates of sheet steels for advanced nuclear reactors, three types of Ni⁻Mo⁻Cr high-strength low alloy (HSLA) steels named as CNST1, CNST2 and CNSS3 were irradiated by 400 keV Fe⁺ with peak fluence to 1.4 × 1014, 3.5 × 1014 and 7.0 × 1014 ions/cm², respectively. The distribution and morphology of the defects induced by the sample preparation method and Fe⁺ irradiation dose were investigated by transmission electron microscopy (TEM) and positron-annihilation spectroscopy (PAS). TEM samples were prepared with two methods, i.e., a focused ion beam (FIB) technique and the electroplating and twin-jet electropolishing (ETE) method. Point defects and dislocation loops were observed in CNST1, CNST2 and CNSS3 samples prepared via FIB. On the other hand, samples prepared via the ETE method revealed that a smaller number of defects was observed in CNST1, CNST2 and almost no defects were observed in CNST3. It is indicated that artifact defects could be introduced by FIB preparation. The PAS S-W plots showed that the existence of two types of defects after ion implantation included small-scale defects such as vacancies, vacancy clusters, dislocation loops and large-sized defects. The S parameter of irradiated steels showed a clear saturation in PAS response with increasing Fe⁺ dose. At the same irradiation dose, higher values of the S-parameter were achieved in CNST1 and CNST2 samples when compared to that in CNSS3 samples. The mechanism and evolution behavior of irradiation-induced defects were analyzed and discussed.

4.
J Biotechnol ; 243: 29-37, 2017 Feb 10.
Article in English | MEDLINE | ID: mdl-28042013

ABSTRACT

Antibody fragments have shown targeted specificity to their antigens, but only modest tissue retention times in vivo and in vitro. Multimerization has been used as a protein engineering tool to increase the number of binding units and thereby enhance the efficacy and retention time of antibody fragments. In this work, we explored the effects of valency using a series of self-assembling polypeptides based on the GCN4 leucine zipper multimerization domain fused to a single-chain variable fragment via an antibody upper hinge sequence. Four engineered antibody fragments with a valency from one to four antigen-binding units of a cytotoxic monoclonal antibody 84 against human embryonic stem cells (hESC) were constructed. We hypothesized that higher cytotoxicity would be observed for fragments with increased valency. Flow cytometry analysis revealed that the trimeric and tetrameric engineered antibody fragments resulted in the highest degree of cytotoxicity to the undifferentiated hESC, while the engineered antibody fragments were observed to have improved tissue penetration into cell clusters. Thus, a trade off was made for the trimeric versus tetrameric fragment due to improved tissue penetration. These results have direct implications for antibody-mediated removal of undifferentiated hESC during regenerative medicine and cell therapy.


Subject(s)
Antibodies, Monoclonal/biosynthesis , Antibodies, Monoclonal/toxicity , Human Embryonic Stem Cells/drug effects , Protein Engineering/methods , Amino Acid Sequence , Antibodies, Monoclonal/chemistry , Antibodies, Monoclonal/genetics , Antibody Affinity , Antigens/chemistry , Chromatography, High Pressure Liquid , Cytotoxicity Tests, Immunologic , Escherichia coli/genetics , Flow Cytometry , Human Embryonic Stem Cells/immunology , Humans , Immunoglobulin Fragments/genetics , Plasmids/genetics , Protein Multimerization/immunology , Recombinant Proteins/chemistry , Recombinant Proteins/immunology , Sequence Analysis, DNA , Single-Chain Antibodies/chemistry
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